TrianglePUBLICATIONS · 23143595
Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing.
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Bibliographic metadata only. No full-text article or abstract is reproduced. Absence of a captured notice is not confirmation that a publication is clear of corrections or retractions.
- Journal
- Nat Genet
- Publication date
- 2012 Dec
- First author
- Richter J
Publication notices
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- relationships
Authors and identifiers
- name
- Richter J
- type
- Author
- name
- Schlesner M
- type
- Author
- name
- Hoffmann S
- type
- Author
- name
- Kreuz M
- type
- Author
- name
- Leich E
- type
- Author
- name
- Burkhardt B
- type
- Author
- name
- Rosolowski M
- type
- Author
- name
- Ammerpohl O
- type
- Author
- name
- Wagener R
- type
- Author
- name
- Bernhart SH
- type
- Author
- name
- Lenze D
- type
- Author
- name
- Szczepanowski M
- type
- Author
Complete bibliographic record and source provenance
- authors
- name
- Richter J
- type
- Author
- name
- Schlesner M
- type
- Author
- name
- Hoffmann S
- type
- Author
- name
- Kreuz M
- type
- Author
- name
- Leich E
- type
- Author
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- Burkhardt B
- type
- Author
- name
- Rosolowski M
- type
- Author
- name
- Ammerpohl O
- type
- Author
- name
- Wagener R
- type
- Author
- name
- Bernhart SH
- type
- Author
- name
- Lenze D
- type
- Author
- name
- Szczepanowski M
- type
- Author
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- document type
- citation
- dois
- 10.1038/ng.2469
- electronic publication date
- display
- 2012 Nov 11
- precision
- day
- year
- 2012
- evidence scope
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- Nat Genet
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- 1546-1718
- issn print
- 1061-4036
- issue
- 12
- name
- Nature genetics
- nlm unique id
- 9216904
- pages
- 1316-20
- volume
- 44
- languages
- eng
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- retrieved at
- 2026-09-09T23:46:52.860383+00:00
- publication date
- display
- 2012 Dec
- precision
- month
- year
- 2012
- publication types
- Journal Article
- Research Support, Non-U.S. Gov't
- record status
- PubMed - indexed for MEDLINE
- schema version
- 1.0
- title
- Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing.
Preserved source evidence · Independent clinical review pending · Not medical advice